Galactosemia history and symptoms: Difference between revisions

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==Overview==
==Overview==
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* [[Diarrhea]]
* [[Diarrhea]]
* [[Failure]] to thrive on [[galactose]] containing foods e.g. [[breast]] milk, formulas containing cow's milk <ref name="pmid7642981">{{cite journal| author=Lewis V, Welch F, Cherry F, Flood E, Marble M| title=Galactosemia: clinical features, diagnosis and management. A case report. | journal=J La State Med Soc | year= 1995 | volume= 147 | issue= 6 | pages= 262-5 | pmid=7642981 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7642981  }} </ref>
* [[Failure]] to thrive on [[galactose]] containing foods e.g. [[breast]] milk, formulas containing cow's milk <ref name="pmid7642981">{{cite journal| author=Lewis V, Welch F, Cherry F, Flood E, Marble M| title=Galactosemia: clinical features, diagnosis and management. A case report. | journal=J La State Med Soc | year= 1995 | volume= 147 | issue= 6 | pages= 262-5 | pmid=7642981 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7642981  }} </ref>
* [[Convulsions]]<ref name="pmid26840667">{{cite journal| author=Sarma MS, Srivastava A, Yachha SK, Poddar U, Mathias A| title=Classical Galactosemia Among Indian Children: Presentation and Outcome from a Pediatric Gastroenterology Center. | journal=Indian Pediatr | year= 2016 | volume= 53 | issue= 1 | pages= 27-31 | pmid=26840667 | doi=10.1007/s13312-016-0784-5 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26840667  }} </ref>


==References==
==References==

Latest revision as of 22:47, 4 July 2022

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sujaya Chattopadhyay, M.D.[2]

Overview

Galactosemia is primarily seen in the neonatal period with a wide range of symptoms.

History

Galactosemia is manifested mostly in the first week of life. Hence, diagnosis is mainly clinical and by newborn screening, some being detected occasionally by family history.[1]

Symptoms [1]

References

  1. 1.0 1.1 Bozkowa K, Zbieg-Sendecka E, Grodzka Z, Cabalska B (1979). "[Clinical and biochemical diagnosis of galactosemia among our cases]". Probl Med Wieku Rozwoj. 8: 63–9. PMID 263527.
  2. Lewis V, Welch F, Cherry F, Flood E, Marble M (1995). "Galactosemia: clinical features, diagnosis and management. A case report". J La State Med Soc. 147 (6): 262–5. PMID 7642981.
  3. Sarma MS, Srivastava A, Yachha SK, Poddar U, Mathias A (2016). "Classical Galactosemia Among Indian Children: Presentation and Outcome from a Pediatric Gastroenterology Center". Indian Pediatr. 53 (1): 27–31. doi:10.1007/s13312-016-0784-5. PMID 26840667.

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